Hostname: page-component-74656f9884-g96k6 Total loading time: 0 Render date: 2026-11-10T11:43:54.818Z Has data issue: false hasContentIssue false
  • English
  • Français

Endoparasite fauna of five Gadiformes fish species from the coast of Chile: host ecology versus phylogeny

Published online by Cambridge University Press:  21 January 2011

R.A. Chávez ,
M.T. González ,
M.E. Oliva  and
I.M. Valdivia
R.A. Chávez
Affiliation:
Instituto de Investigaciones Oceanológicas, Facultad de Recursos del Mar, Universidad de Antofagasta, PO Box 170, Antofagasta, Chile
M.T. González
Affiliation:
Instituto de Investigaciones Oceanológicas, Facultad de Recursos del Mar, Universidad de Antofagasta, PO Box 170, Antofagasta, Chile
M.E. Oliva*
Affiliation:
Instituto de Investigaciones Oceanológicas, Facultad de Recursos del Mar, Universidad de Antofagasta, PO Box 170, Antofagasta, Chile
I.M. Valdivia
Affiliation:
Instituto de Investigaciones Oceanológicas, Facultad de Recursos del Mar, Universidad de Antofagasta, PO Box 170, Antofagasta, Chile
*
*Fax: 56-55-637804 E-mail: meoliva@uantof.cl
Rights & Permissions [Opens in a new window]

Abstract

The aims of the present study were to compare, using multivariate analyses, the degree of similarity of the endoparasite fauna of five fish species belonging to the order Gadiformes: Merluccius gayi, Merluccius australis, Macruronus magellanicus (Gadoidei) and Micromesistius australis and Nezumia pulchella (Macrouroidei), from the southern and central Chilean coast, and to evaluate whether the composition of the endoparasite fauna was determined by phylogenetic or ecological relationships. We employed our database of Merluccius australis, M. magellanicus and Micromesistius australis, which was complemented with published information for M. magellanicus, Merluccius australis, Micromesistius australis, M. gayi and N. pulchella. A higher number of endoparasite species was recorded for Merluccius australis, Micromesistius australis and M. magellanicus, namely Anisakis sp. and Hepatoxylon trichiuri, which is the most prevalent parasite among these hosts. Aporocotyle wilhelmi and Hysterothylacium sp. were detected only in M. gayi, whereas Lepidapedon sp. was found exclusively in N. pulchella. These results suggest that fish ecology rather than host phylogeny was the most important factor for the determination of similarity in parasite composition. This result could be explained by the similar trophic patterns of hosts and by the predominance of generalist larval species among these fish parasite communities.

Information

Type
Research Papers
Information
Journal of Helminthology , Volume 86 , Issue 1 , March 2012 , pp. 10 - 15
Copyright
Copyright © Cambridge University Press 2011

Introduction

The composition of parasite communities is affected by, among other factors, the result of the interactions between their evolutionary history and the ecological characteristics of the hosts (Poulin, Reference Poulin1995). During their evolutionary history, hosts lose and/or acquire parasites due to the speciation of native parasites or the acquisition of new parasite species from other hosts (Poulin & Rohde, Reference Poulin and Rohde1997). The ecological characteristics associated with the host, such as diet, habitat and niche position, have a great influence on the composition and structure of the parasite communities (Esch et al., 1990; Poulin, Reference Poulin1995). Moreover, host geographic range is a main factor affecting the interchanges of parasite species that are phylogenetically related (Poulin & Morand, Reference Poulin and Morand1999; González & Oliva, Reference González and Oliva2006). Similarly, it has been demonstrated that depth and temperature both affect the parasite communities of fish (Rohde et al., Reference Rohde, Hayward and Heap1995; Oliva et al., Reference Oliva, Gonzalez and Acuña2004).

Studies of parasite communities that do not account for phylogeny may provide inaccurate results (Brooks, Reference Brooks1980). Studies that analyse the determinants of parasite communities of related hosts show that phylogenetic relationships can confuse the real relationships between host ecology and community parasite richness (Poulin & Rohde, Reference Poulin and Rohde1997). However, few studies have evaluated the importance of ecological and phylogenetic factors of the host simultaneously as determinants of parasite communities (Bush et al., 1990; Poulin, Reference Poulin1996, Reference Poulin2010; Muñoz et al., Reference Muñoz, Grutter and Cribb2006), and those studies have provided contradictory results concerning the relationship between parasitological descriptors and ecological variables and/or host phylogeny. Therefore, additional studies are needed to determine whether these trends in the determination of parasite communities are consistent when the ecology and phylogeny of the host are considered.

The aims of the present study were to compare, using multivariate analyses, the degree of similarity of the endoparasite fauna of five fish species belonging to the order Gadiformes: three representatives of the suborder Gadoidei (Merluccius gayi, Merluccius australis (Merlucciidae), Macruronus magellanicus (Macrouronidae)) and two representatives of the suborder Macrouroidei (Nezumia pulchella (Macrouridae) and Micromesistius australis (Gadidae)), and to evaluate whether endoparasite compositions were mainly influenced by phylogenetic or by ecological relationships (e.g. niche dimensions such as diet, depth, latitude or habitat). Two host species (M. gayi and N. pulchella) share latitudinal and bathymetric distributions along the northern Chilean coast, whereas the other three host species (Merluccius australis, M. magellanicus and Micromesistius australis) are distributed along the central-southern Chilean coast (Froese & Pauly, Reference Froese and Pauly2010). As stated by Lillo et al. (Reference Lillo, Céspedes, Ojeda, Balbontín, Bravo, Saavedra, Barbieri and Vera2005) and Saavedra et al. (Reference Saavedra, Correa, Céspedes, Ojeda, Adarme, Días, Oliva and Rojas2006), these species share similar trophic patterns.

Materials and methods

We used our own database comprising M. magellanicus, Merluccius australis and Micromesistius australis, which were caught in 2006 by an industrial fishery from southern Chile (44°S and 45°S). Additionally, our database was complemented with published information for M. magellanicus, Merluccius australis, Micromesistius australis, M. gayi and N. pulchella (table 1). The latitudinal and bathymetric ranges and sizes for each species are presented in table 2.

Table 1

Prevalence (P) and mean intensity of infection (MI) of endoparasites of five Gadiformes fish species off the Chilean coast.

* Larval stages.

Table 2

Number of analysed fish (n), fish size range (mean±SD), latitudinal range and bathymetric range in gadiform fish species from Chile.

Sources: (1) This study; (2) Fernández (Reference Fernández1985); (3) George-Nascimento & Arancibia (Reference George-Nascimento and Arancibia1994); (4) González (2005) ; (5) George-Nascimento (Reference George-Nascimento1996); (6) Oliva (Reference Oliva2001); (7) Niklitschek et al. (Reference Niklitschek, Canales, Ferrada, Galleguillos, George-Nascimento, Hernandez, Herranz, Lafon, Roa and Toledo2009); (8) Salinas et al. (Reference Salinas, González and Acuña2008).

* From Froese & Pauly (Reference Froese and Pauly2010).

For each parasite species, the prevalence and mean intensity of infection were calculated according to Bush et al. (Reference Bush, Lafferty, Lotz and Shostak1997). Cluster analyses (based on the Bray–Curtis similarity and simple linkage algorithm) were used to determine whether the endoparasite composition (prevalence and intensity of infection) among host species was similar. Correspondence analyses were then employed to evaluate the host–parasite associations. All multivariate analyses were performed using Statistica 6.0 software (StatSoft Inc., Tulsa, Oklahoma, USA).

Results

The host species N. pulchella showed the narrowest latitudinal range, whereas Merluccius australis, M. magellanicus and Micromesistius australis demonstrated overlapping latitudinal distributions (table 2). Twenty endoparasite species were detected in the studied hosts. Of these species, seven were in the larval stages, and several parasite species were common among the host species. The larval parasites Anisakis sp. and Hepatoxylon trichiuri demonstrated a higher prevalence of infection in Merluccius australis, Micromesistius australis and M. magellanicus (table 1). There was no relationship between the sample size and parasite richness (r 2 = 0.107, P>0.20).

The cluster analysis based on parasite prevalence (fig. 1) included Micromesistius australis and M. magellanicus in a clade with 50% similarity; Merluccius australis was included in this clade with a similarity of 49% and M. gayi with a similarity of 36%. Finally, N. pulchella demonstrated a parasite similarity of only 23% with the other four host species. The cluster analysis based on the mean intensity of infection (fig. 2) revealed the same pattern.

Fig. 1

Cluster analyses based on prevalence of infection of endoparasite fauna of five Gadiformes species. Code for host species: Nezumia pulchella (NEPU), Merluccius gayi (MEGA), Merluccius australis (MEAU), Micromesistius australis (MIAU) and Macruronus magellanicus (MAMA).

Fig. 2

Cluster analyses based on mean intensities of infection of endoparasite fauna of five Gadiformes species. Code for species as in fig. 1.

The correspondence analysis based on prevalence (fig. 3) demonstrated significant differences in endoparasite composition among the host species (χ2 = 630.07, df = 76, P < 0.001); 66.5% of the variation was explained by the first two dimensions (39% and 27.5% for the first and second dimensions, respectively). Most parasites were associated with Merluccius australis and Micromesistius australis. However, Aporocotyle wilhelmi and Hysterothylacium sp. were strongly associated with M. gayi. Similarly, Elytrophalloides oatesi, Gonocerca phycidis and Cucullanus sp. were only associated with M. magellanicus, whereas Lepidapedon sp. was present only in N. pulchella (fig. 3).

Fig. 3

Correspondence analysis based on prevalence of infection: Nezumia pulchella (Nepu), Merluccius gayi (Mega), Merluccius australis (Meau), Micromesistius australis (Miau) and Macruronus magellanicus (Mama). 1, Aporocotyle wilhelmi; 2, Aporocotyle australis; 3, Derogenes varicus; 4, Elytrophalloides oatesi; 5, Gonocerca phycidis; 6, Hemiuridae gen sp.; 7, Lepidapedon sp.; 8, Anisakis sp.; 9, Ascarophis sp.; 10, Pseudoterranova sp.; 11, Contracaecum sp.; 12, Hysterothylacium sp.; 13, Hysterothylacium aduncum; 14, Cucullanus sp.; 15, Corynosoma sp.; 16, Pseudophyllidea gen sp.; 17: Hepatoxylon trichiuri; 18, Clestobothrium crassiceps; 19, Grillotia heptanchi; 20, Diphyllobotrium sp.

The correspondence analysis based on the mean intensity of infection (fig. 4) also showed significant differences in endoparasite composition among the host species (χ2 = 1812.1, df = 76, P < 0.001); 68% of the variation was explained by the first two dimensions (38.6% and 29.7% for the first and second dimensions, respectively). Several endoparasites were associated with Merluccius australis, Micromesistius australis, M. magellanicus and M. gayi (fig. 4).

Fig. 4

Correspondence analyses based on mean intensity of infection. Code for host species and parasite species as in fig. 3.

Discussion

Several studies have evaluated the role of ecological factors (e.g. niche dimensions such as diet, depth, latitude and habitat) on the structure and parasite richness of fishes (Aldana et al., Reference Aldana, Pulgar, Ogalde and Ojeda2002; Muñoz et al., Reference Muñoz, Valdebenito and George-Nascimento2002). However, studies investigating the relationship between parasite descriptors and ecological variables of the host, in particular those including phylogeny, are scarce (Poulin & Rohde, Reference Poulin and Rohde1997; Morand et al., Reference Morand, Cribb, Kulbicki, Rigby, Chauvet, Dufour, Faliex, Galzin, Lo, Lo-Yat, Pichelin and Sasal2000; Muñoz et al., Reference Muñoz, Grutter and Cribb2006). Specifically, the endoparasite communities of fishes can be determined by the feeding habits of the host (for instance, specialist versus generalist predators), changes in their ontogenetic feeding, and the availability of different prey (intermediary hosts) in a given environment (Poulin, Reference Poulin1995). The host species Micromesistius australis and M. magellanicus, which belong to different suborders in the Gadiformes, show greater similarity in their endoparasite compositions, which can be best explained by their similar trophic patterns instead of by phylogeny. Micromesistius australis, M. magellanicus and Merluccius australis are related trophically, because they feed mainly on the same species of myctophid fish (e.g. Lampanyctus sp.) and crustacean (Pasiphaea doffleini) (Lillo et al., Reference Lillo, Céspedes, Díaz and Ojeda2004, Reference Lillo, Céspedes, Ojeda, Balbontín, Bravo, Saavedra, Barbieri and Vera2005; Saavedra et al., Reference Saavedra, Correa, Céspedes, Ojeda, Adarme, Días, Oliva and Rojas2006). This similarity in diet agrees well with the similarity of the endoparasite fauna of Micromesistius australis and M. magellanicus, which in turn is supported by cluster and correspondence analyses (figs 1–4), emphasizing the higher prevalence of H. trichiuri and Anisakis sp. in these three host fishes. The latter parasite can be transmitted to Merluccius australis via the ingestion of juveniles of M. magellanicus, their main prey (Lillo et al., Reference Lillo, Céspedes, Ojeda, Balbontín, Bravo, Saavedra, Barbieri and Vera2005), which is an intermediate host of Anisakis sp. (Riffo & George-Nascimento, Reference Riffo and George-Nascimento1992). The infection of Micromesistius australis by Anisakis sp. could be explained by the consumption of intermediate hosts (Crustacea) (Sakanari & McKerrow, Reference Sakanari and McKerrow1989). The cestode H. trichiuri is a common parasite of merluccid fish (Mladineo, Reference Mladineo2006). This cestode can infect all three hosts through the ingestion of larval stages harboured by crustaceans (Vásquez-López et al., 2001). The similar trophic patterns of two Gadoidei (Merluccius australis, M. magellanicus) and one Macrouroidei (Micromesistius australis) are caused by their spatial overlap (both latitudinal and bathymetric). In contrast, the distribution of M. gayi overlaps those of the other three species only within a narrow latitudinal range, 28°S–47°S (Aguayo, Reference Aguayo, Alheit and Pitcher1995); this host species demonstrates distinct feeding habits, with its most important prey being the crustaceans Pterygosquilla armata, Pleuroncodes monodon, Cerviminuda johni and Euphausia mucronata, the fishes Engraulis ringens and Strangomera bentincki and other M. gayi (Arancibia & Fuentealba, Reference Arancibia and Fuentealba1993). On the other hand, N. pulchella overlaps with M. gayi both latitudinally and bathymetrically between 20°S and 33°S (Sielfeld & Vargas, Reference Sielfeld and Vargas1996). This spatial overlap is not reflected in the parasite composition of these two fish species, as shown by cluster and correspondence analyses (figs 3 and 4). The lack of similarity between endoparasite fauna of N. pulchella and M. gayi could be explained by the digenean Aporocotyle wilhelmi, which is a parasite specific to M. gayi (Villalba & Fernández, Reference Villalba and Fernández1986). However, the most important endoparasite species of N. pulchella (Macrouridae) is the digenean Lepidapedon sp., which is a common parasite of Gadiformes species (Bray & des Clers, Reference Bray and des Clers1992).

The phylogenetic information provided by comparative analysis avoids confusing effects among analysed ecological variables (Harvey & Pagel, Reference Harvey and Pagel1991). Phylogenetic effects could be hidden by ecological effects, except in the presence of strong host ecological effects and high probabilities of acquiring or losing parasites, or in the case of marked changes in ecological characteristics during speciation events (Vickery & Poulin, Reference Vickery and Poulin1998). According to Morand et al. (Reference Morand, Cribb, Kulbicki, Rigby, Chauvet, Dufour, Faliex, Galzin, Lo, Lo-Yat, Pichelin and Sasal2000), host phylogenetic relationships have a strong influence on patterns of parasite richness. However, a consistent pattern explaining the variations in endoparasite composition and richness among fish species of Labridae (Cheiliniae) has not been observed, unless the species are phylogenetically related and present very similar diets and body sizes (Muñoz et al., Reference Muñoz, Grutter and Cribb2006). These observations suggest that the phylogenetic relationships of hosts do not have a significant effect on the structure of their parasite communities, and thus, the mixed effects of host descriptors (diet, weight) and phylogeny are the main contributors to endoparasite composition. Recently, Poulin (Reference Poulin2010) suggested that similarity of parasite fauna decreases with the phylogenetic distance of the host species. In the present study, the results of multivariate analyses (figs 1–4) supported the observation that the fish species most closely related phylogenetically (Merluccius gayi and Merluccius australis) did not show greater parasite fauna similarities. In a similar way, the two species belonging to the suborder Macrouroidei (M. magellanicus and N. pulchella), as defined by Roa-Varón & Ortí (Reference Roa-Varón and Ortí2009), show the higher divergence in the composition of their parasite fauna. Moreover, our results suggest that the most closely related parasite fauna is shared by Micromesistius australis and M. magellanicus – species that belong to different suborders in the Gadiformes. Those findings might be explained by the latitudinal/bathymetric segregation of these species and, consequently, the differential prey availabilities, indicating that the composition of the endoparasite fauna is mainly influenced by feeding habits (predator–prey relationships).

In summary, among the Gadiformes species studied herein, the high degree of endoparasite similarity was determined principally by their ecological characteristics (trophic overlap); consequently, phylogenetic relationships could play a secondary role in the determination of their endoparasite fauna. Nevertheless, and similarly to the results reported by Muñoz et al. (Reference Muñoz, Grutter and Cribb2006), the Gadiformes fish species described herein harbour mainly generalist endoparasites (Anisakis sp., H. trichiuri, Derogenes varicus), which infect several demersal fishes (Genypterus spp., Dissostichus eleginoides, Hippoglossina macrops, among others) (George-Nascimento & Huet, Reference George-Nascimento and Huet1984; Oliva et al., Reference Oliva, Gonzalez and Acuña2004, Reference Oliva, Fernández, Oyarzun and Murillo2008). In addition, there is a possibility that our results could be biased, because generalist larval species such as H. trichiuri, Anisakis sp. and Pseudoterranova sp. could be different species that are morphologically similar, a finding that has been demonstrated genetically for some anisakid species (Mattiucci & Nascetti, Reference Mattiucci and Nascetti2007). Therefore, molecular studies may be necessary to identify such species and to evaluate conclusively the effects of ecological and phylogenetic factors on the composition of endoparasite communities in Gadiformes fish species.

References

Aguayo, M. (1995) Biology and fisheries of Chilean hakes (M. gayi and M. australis). pp. 305–338in Alheit, J. & Pitcher, T.J. (Eds) Biology, fisheries and markets. London, Chapman & Hall.Google Scholar
Aldana, M., Pulgar, J.M., Ogalde, F. & Ojeda, F.P. (2002) Morphometric and parasitological evidence for ontogenetic and geographical dietary shifts in intertidal fishes. Bulletin of Marine Science 70, 55–74.Google Scholar
Arancibia, H. & Fuentealba, M. (1993) Análisis de la alimentación de Merluccius gayi gayi (Guichenot, 1848) de Chile central, en el largo plazo. Biología Pesquera 22, 5–11.Google Scholar
Bray, R.A. & des Clers, S.A. (1992) Multivariate analyses of metrical features in the Lepidapedon elongatum (Lebour, 1908) species-complex (Digenea: Lepocreadiidae) in deep and shallow water gadiform fishes of the NE Atlantic. Systematic Parasitology 21, 223–232.CrossRefGoogle Scholar
Brooks, D.R. (1980) Allopatric speciation and non-interactive parasite community structure. Systematic Zoology 29, 192–203.CrossRefGoogle Scholar
Bush, A.O., Aho, J.M. & Kennedy, C.R. (1990) Ecological versus phylogenetic determinants of helminth parasite community richness. Evolutionary Ecology 4, 1–20.CrossRefGoogle Scholar
Bush, A.O., Lafferty, K.D., Lotz, J.M. & Shostak, A.W. (1997) Parasitology meets ecology on its own terms: Margolis et al. revisited. Journal of Parasitology 83, 575–580.CrossRefGoogle Scholar
Esch, G.W., Bush, A.O. & Aho, J.M. (1990) Parasite communities: Patterns and process. London, Chapman & Hall.Google Scholar
Fernández, J. (1985) Estudio parasitológico de Merluccius australis (Hutton, 1872) (Pisces: Merlucciidae): Aspectos sistemáticos, estadísticos y zoogeográficos. Boletín de la Sociedad de Biología de Concepción 56, 31–41.Google Scholar
Froese, R. & Pauly, D. (2010) FishBase. World Wide Web electronic publication, available athttp://www.fishbase.org>, version (accessed September 2010).,+version+(accessed+September+2010).>Google Scholar
George-Nascimento, M. (1996) Populations and assemblages of parasites in hake, Merluccius gayi, from the southern Pacific Ocean: stock implications. Journal of Fish Biology 48, 557–568.CrossRefGoogle Scholar
George-Nascimento, M. & Arancibia, H. (1994) La fauna parasitaria y la morfometría de la merluza austral Merluccius australis (Hutton) como indicadoras de unidades de stock. Biología Pesquera 23, 31–47.Google Scholar
George-Nascimento, M. & Huet, B. (1984) Una aproximación ecológica al estudio del parasitismo en el congrio negro Genypterus maculatus (Tschudi) (Pisces: Ophidiidae). Biología Pesquera 13, 23–30.Google Scholar
González, L. (2005) Diagnostico Merluza del Sur y Congrio Dorado en aguas interiores de la XII Región. Informe Final Fondema Magallanes y Antártica Chilena. Technical report. Available athttp://164.77.209.178/gorenew/ESTUDIOS/Archivos/Archivo%20Estudios/20196777/Resumen_MerluzaYCongrio.pdf (accessed 30 June 2010).Google Scholar
González, M.T. & Oliva, M.E. (2006) Similarity and structure of the ectoparasite communities of rockfish species from the southern Chilean coast in a temporal scale. Parasitology 133, 335–343.CrossRefGoogle Scholar
Harvey, P.H. & Pagel, H. (1991) The comparative method in evolutionary biology. Oxford, Oxford University Press.CrossRefGoogle Scholar
Lillo, S., Céspedes, R., Díaz, E. & Ojeda, V. (2004) Evaluación Hidroacústica del Stock parental de merluza de tres aletas en su unidad de pesquería, año 2003. Technical report FIP 2003-10. pp. 32–35. Available atwww.fip.cl (accessed 30 June 2010).Google Scholar
Lillo, S., Céspedes, R., Ojeda, V., Balbontín, F., Bravo, R., Saavedra, A., Barbieri, M.A. & Vera, C. (2005) Evaluación del stock desovante de merluza del Sur y merluza de cola en la zona Sur Austral año 2004. Technical report FIP 2004-07. pp. 60–63. Available atwww.fip.cl (accessed 30 June 2010).Google Scholar
Mattiucci, S. & Nascetti, G. (2007) Advances and trends in the molecular systematics of anisakid nematodes, with implications for their evolutionary ecology and host–parasite co-evolutionary processes. Advances in Parasitology 66, 47–138.CrossRefGoogle Scholar
Mladineo, I. (2006) Hepatoxylon trichiuri (Cestoda: Trypanorhyncha) plerocercoids in cage-reared northern bluefin tuna, Thunnus thynnus (Osteichthyes: Scombridae). Acta Adriatica 47, 79–83.Google Scholar
Morand, S., Cribb, T.H., Kulbicki, M., Rigby, M.C., Chauvet, C., Dufour, V., Faliex, E., Galzin, R., Lo, C.M., Lo-Yat, A., Pichelin, S. & Sasal, P. (2000) Endoparasite species richness of New Caledonian butterfly fishes: host density and diet matter. Parasitology 121, 65–73.CrossRefGoogle ScholarPubMed
Muñoz, G., Valdebenito, V. & George-Nascimento, M. (2002) La dieta y la fauna de parásitos metazoos del torito Bovichthys chilensis Regan 1914 (Pisces:Bovichthydae) en la costa de Chile centro-sur: variaciones geográficas y ontogenéticas. Revista Chilena de Historia Natural 75, 661–671.CrossRefGoogle Scholar
Muñoz, G., Grutter, R.A. & Cribb, T.H. (2006) Endoparasite communities of five fish species (Labridae: Cheilininae) from Lizard Island: how important is the ecology and phylogeny of the hosts? Parasitology 132, 363–374.CrossRefGoogle ScholarPubMed
Niklitschek, E., Canales, C., Ferrada, S., Galleguillos, R., George-Nascimento, M., Hernandez, E., Herranz, C., Lafon, A., Roa, R. & Toledo, P. (2009) Unidades Poblacionales de Merluza de Tres Aletas (Micromesistius australis). Technical report FIP. pp. 70–76. Available atwww.fip.cl (accessed 30 June 2010).Google Scholar
Oliva, M.E. (2001) Metazoan parasites of Macruronus magellanicus from southern Chile as biological tags. Journal of Fish Biology 58, 1617–1622.CrossRefGoogle Scholar
Oliva, M.E., Gonzalez, M.T. & Acuña, E. (2004) Metazoan parasite fauna as biological tag for the habitat of the Flounder, Hippoglossina macrops from Northern Chile, in a depth gradient. Journal of Parasitology 90, 1374–1377.CrossRefGoogle Scholar
Oliva, M.E., Fernández, I., Oyarzun, C. & Murillo, C. (2008) Metazoan parasites of the stomach of Dissostichus eleginoides Smitt 1898 (Pisces: Notothenidae) from southern Chile: A tool for stock discrimination? Fisheries Research 91, 119–122.CrossRefGoogle Scholar
Poulin, R. (1995) Phylogeny, ecology, and the richness of parasite communities in vertebrates. Ecological Monographs 65, 283–302.CrossRefGoogle Scholar
Poulin, R. (1996) Richness, nestedness, and randomness in parasite infracommunity structure. Oecologia 105, 545–551.CrossRefGoogle ScholarPubMed
Poulin, R. (2010) Decay of similarity with host phylogenetic distance in parasite faunas. Parasitology 137, 733–741.CrossRefGoogle ScholarPubMed
Poulin, R. & Morand, S. (1999) Geographical distances and the similarity among parasite communities of conspecific host populations. Parasitology 119, 369–374.CrossRefGoogle ScholarPubMed
Poulin, R. & Rohde, K. (1997) Comparing the richness of metazoan ectoparasite communities of marine fishes: controlling for host phylogeny. Oecologia 110, 278–283.CrossRefGoogle ScholarPubMed
Riffo, R. & George-Nascimento, M. (1992) Variaciones de la abundancia de larvas de Anisakis sp. y Hysterothylacium sp. (Nematoda: Anisakidae) en la merluza de cola Macruronus magellanicus Lonnberg 1862: La importancia del sexo, tamaño corporal y dieta del hospedador. Estudios Oceanológicos 11, 79–84.Google Scholar
Roa-Varón, A. & Ortí, G. (2009) Phylogenetic relationships among families of Gadiformes (Teleostei, Paracanthopterygii) based on nuclear and mitochondrial data. Molecular Phylogenetics and Evolution 52, 688–704.CrossRefGoogle ScholarPubMed
Rohde, K., Hayward, C. & Heap, M. (1995) Aspect of the ecology of metazoan ectoparasites of fishes. International Journal for Parasitology 25, 945–970.CrossRefGoogle ScholarPubMed
Saavedra, A., Correa, V., Céspedes, R., Ojeda, V., Adarme, L., Días, E., Oliva, J. & Rojas, P. (2006) Evaluación hidroacústica del Stock parental de merluza de tres aletas en su unidad de pesquería año, 2005. Technical report FIP 2005-06. pp. 71–72. Available atwww.fip.cl (accessed 30 June 2010).Google Scholar
Sakanari, A.J. & McKerrow, H.M. (1989) Anisakiasis. Clinical Microbiology Reviews 2, 278–284.CrossRefGoogle ScholarPubMed
Salinas, X., González, M.T. & Acuña, E. (2008) Metazoan parasites of the thumb grenadier Nezumia pulchella, from the south-eastern Pacific of Chile, and their use for discrimination of host populations. Journal of Fish Biology 73, 683–691.CrossRefGoogle Scholar
Sielfeld, W. & Vargas, M. (1996) Composición y estructura de la ictiofauna demersal en la zona norte de Chile. Investigaciones Marinas 24, 3–17.CrossRefGoogle Scholar
Vázquez-López, C., Armas-Serra, C. & Rodríguez-Caabeiro, F. (2001) Gymnorhynchus gigas: Taxonomía, morfología, biología y aspectos sanitarios. Analecta veterinaria 2, 38–49.Google Scholar
Vickery, W.L. & Poulin, R. (1998) Parasite extinction and colonization and the evolution of parasite communities: a simulation study. International Journal for Parasitology 28, 727–737.CrossRefGoogle ScholarPubMed
Villalba, C. & Fernández, J. (1986) Dos nuevas especies de trematodos parásitos de peces marinos de Chile. Parasitologia al Dia 10, 45–51.Google Scholar
Figure 0

Table 1 Prevalence (P) and mean intensity of infection (MI) of endoparasites of five Gadiformes fish species off the Chilean coast.

Figure 1

Table 2 Number of analysed fish (n), fish size range (mean±SD), latitudinal range and bathymetric range in gadiform fish species from Chile.

Figure 2

Fig. 1 Cluster analyses based on prevalence of infection of endoparasite fauna of five Gadiformes species. Code for host species: Nezumia pulchella (NEPU), Merluccius gayi (MEGA), Merluccius australis (MEAU), Micromesistiusaustralis (MIAU) and Macruronus magellanicus (MAMA).

Figure 3

Fig. 2 Cluster analyses based on mean intensities of infection of endoparasite fauna of five Gadiformes species. Code for species as in fig. 1.

Figure 4

Fig. 3 Correspondence analysis based on prevalence of infection: Nezumia pulchella (Nepu), Merluccius gayi (Mega), Merluccius australis (Meau), Micromesistiusaustralis (Miau) and Macruronus magellanicus (Mama). 1, Aporocotyle wilhelmi; 2, Aporocotyle australis; 3, Derogenes varicus; 4, Elytrophalloides oatesi; 5, Gonocerca phycidis; 6, Hemiuridae gen sp.; 7, Lepidapedon sp.; 8, Anisakis sp.; 9, Ascarophis sp.; 10, Pseudoterranova sp.; 11, Contracaecum sp.; 12, Hysterothylacium sp.; 13, Hysterothylaciumaduncum; 14, Cucullanus sp.; 15, Corynosoma sp.; 16, Pseudophyllidea gen sp.; 17: Hepatoxylon trichiuri; 18, Clestobothrium crassiceps; 19, Grillotia heptanchi; 20, Diphyllobotrium sp.

Figure 5

Fig. 4 Correspondence analyses based on mean intensity of infection. Code for host species and parasite species as in fig. 3.